Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.
- NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_assertion description "[The deletion of the p16(INK4A)/p14(ARF) or mutation of p53, key regulatory protein of cell cycle checkpoint in G1/S progression, found in five of the eight pediatric patients suggests that in these cases genetic lesions associated with HTLV-I infection may predispose for an early onset of leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.
- NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_assertion evidence source_evidence_literature NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.
- NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_assertion SIO_000772 11755465 NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.
- NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_assertion wasDerivedFrom befree-20140225 NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.
- NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_assertion wasGeneratedBy ECO_0000203 NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP532301.RA2sxa9GYCNZs4yB7Y7Ry8Klz0p4rGntC1DwxpWOZZ1Dk130_provenance.